Human tnfrsf25 antibody

ABSTRACT

Antibodies and antigen binding fragments that bind specifically to TNFRSF25 are provided herein. Methods for using the antibodies and antigen binding fragments to, for example, stimulate proliferation of human T cells (e.g., CD8+ T cells) and to treat cancer patients also are provided.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. application Ser. No.15/964,770, filed on Apr. 27, 2018 (now U.S. Pat. No. 10,683,358), whichis a continuation of U.S. application Ser. No. 15/527,430, filed on Nov.17, 2015 (now U.S. Pat. No. 9,982,057), which is a National Stage Entryof PCT/US2015/061082, filed on Nov. 17, 2015, which claims benefit ofpriority from U.S. Provisional Application No. 62/134,740, filed on Mar.18, 2015, and U.S. Provisional Application No. 62/080,694, filed on Nov.17, 2014, all of which are incorporated herein by reference in theirentireties.

TECHNICAL FIELD

This document relates to antibodies and antigen binding fragmentsthereof that bind specifically to TNFRSF25, and to methods for using theantibody and antigen binding fragments to, for example, stimulateproliferation of human T cells (e.g., CD8+ T cells), and to treat cancerpatients.

BACKGROUND

Tumor necrosis factor receptor superfamily member 25 (TNFRSF25) is amember of the TNF-receptor superfamily that is preferentially expressedby activated and antigen-experienced T lymphocytes. TNFRSF25 isactivated by the TL1A (TNFSF15) ligand, which is rapidly upregulated inantigen presenting cells and in some endothelial cells followingToll-Like Receptor or Fc receptor activation. TNFRSF25 can stimulateNF-kappa B activity, and also can stimulate caspase activation toregulate cell apoptosis (Bodmer et al., Immunity 6(1):79-88, 1997; andKitson et al., Nature 384(6607):372-375, 1996). Alternative splicingproduces multiple distinct isoforms of TNFRSF25, most of which arepotentially secreted molecules. Alternative splicing of the TNFRSF25gene in B and T cells encounters a program change upon T-cellactivation, which predominantly produces full-length, membrane boundisoforms, and is thought to be involved in controlling lymphocyteproliferation induced by T-cell activation.

Activation of TNFRSF25 is dependent on previous engagement of the T cellreceptor. After binding to TL1A, TNFRSF25 signaling increases thesensitivity of T cells to endogenous IL-2, and enhances T cellproliferation. Since activation of TNFRSF25 is T cell receptordependent, the activity of TNFRSF25 in vivo is specific to T cells thatare encountering cognate antigen. At rest, and when there is nounderlying autoimmunity, the majority of T cells that regularlyencounter cognate antigen are FoxP3+ regulatory T cells. Stimulation ofTNFRSF25, in the absence of any other exogenous signals, stimulateshighly specific proliferation of FoxP3+ regulatory T cells from abaseline of 8-10% of all CD4+ T cells to 35-40% of all CD4+ T cells,within five days (Schreiber et al., J Clin Invest 120(10):3629-3640,2010). Therapeutic agonists of TNFRSF25 can be used to stimulate Tregexpansion, which can reduce inflammation in experimental models ofasthma, allogeneic solid organ transplantation, and ocular keratitis(Schreiber et al., supra; Reddy et al., J Virol 86(19):10606-10620,2012; and Wolf et al., Transplantation 94(6):569-574, 2012). Similarly,because TNFRSF25 activation is antigen dependent, costimulation ofTNFRSF25 together with an autoantigen or with a vaccine antigen can leadto exacerbation of immunopathology or enhanced vaccine-stimulatedimmunity, respectively (Schreiber et al., J Immunol 189(7):3311-3318,2010).

SUMMARY

This document provides agonistic human and humanized TNFRSF25 specificmonoclonal antibodies, and antigen binding fragments thereof. Alsoprovided herein are methods for, inter alia, using the antibodies andantigen binding fragments to stimulate proliferation of human T cells,as well as methods for using the antibodies and antigen bindingfragments in the treatment of human cancer patients (e.g., byadministering an amount of an antibody or antigen binding fragment thatis effective to stimulate proliferation of CD8+ T cells).

In one aspect, this document features an isolated heavy chain variableregion polypeptide that binds specifically to TNFRSF25, where thepolypeptide includes heavy chain CDR1, CDR2, and CDR3 sequences, wherethe CDR1 sequence is GFTFSNHDLN (SEQ ID NO:4), the CDR2 sequence isYISSASGLISYADAVRG (SEQ ID NO:6); and (c) the CDR3 sequence isDPPYSGLYALDF (SEQ ID NO:8). The isolated heavy chain variable regionpolypeptide can further include variable region heavy chain framework(FW) sequences juxtaposed between the heavy chain CDRs according to theformula (FW1)-(CDR1)-(FW2)-(CDR2)-(FW3)-(CDR3)-(FW4). The heavy chainframework sequences can be human. In some embodiments, the isolatedheavy chain variable region polypeptide can be combination with a lightchain variable region polypeptide comprising light chain CDR1, CDR2, andCDR3 sequences, wherein the CDR1 sequence is TLSSELSSYTIV (SEQ IDNO:11), the CDR2 sequence is LKSDGSHSKGD (SEQ ID NO:13), and the CDR3sequence is GAGYTLAGQYGWV (SEQ ID NO:15). Variable region light chainframework (FW) sequences can be juxtaposed between the light chain CDRsaccording to the formula (FW1)-(CDR1)-(FW2)-(CDR2)-(FW3)-(CDR3)-(FW4).The light chain framework sequences can be human.

In another aspect, this document features an isolated anti-TNFRSF25antibody or antigen binding fragment thereof, where the antibody orantibody fragment contains (i) a heavy chain variable region sequencecontaining the amino acid sequence set forth in SEQ ID NO:1 or the aminoacid sequence of SEQ ID NO:1 with no more than 12 total amino acidsubstitutions, and (ii) a light chain variable region sequencecontaining the amino acid sequence of SEQ ID NO:2 or the amino acidsequence of SEQ ID NO:2 with no more than 11 total amino acidsubstitutions. The antibody or antigen binding fragment can furtherinclude a human constant region (e.g., a constant region selected fromthe group consisting of human IgG1, IgG2, IgG3, and IgG4), or a murineconstant region (e.g., a constant region selected from the groupconsisting of murine IgG1, IgG2A, IgG2B, and IgG3). The antibody orantigen binding fragment can have reduced or minimal effector function.The antibody or antigen binding fragment can bind to human TNFRSF25 withan affinity of about 5 nM. The antibody or antigen binding fragment canbe capable of increasing proliferation of human, murine, or macaque Tcells in vitro or in vivo (e.g., wherein the proliferation of the T cellis increased by at least 20%, as determined by flow cytometry analysisof antigen specific T cells). Administration of the antibody or antigenbinding fragment to a subject at a dose of about of 0.1 mg/kg to about50 mg/kg can lead to stimulation of T cell proliferation in the subject,and/or to increased tumor cell apoptosis in the subject.

This document also features a pharmaceutical composition containing apharmaceutically acceptable carrier and an antibody or antigen bindingfragment as described herein.

In addition, this document features an article of manufacture containinga pharmaceutical composition as provided herein and at least oneadditional agent for treating cancer. The at least one additional agentcan include, for example, an agent that targets CTLA-4, PD-1, PD-L1,LAG-3, Tim-3, TNFRSF4, TNFRSF9, TNFRSF18, CD27, CD39, CD47, CD73, orCD278, an A2A receptor antagonist, a TGF-beta antagonist, a B7 familycostimulatory molecule, a TNF receptor superfamily costimulatorymolecule, a vaccine composition, chimeric antigen receptor-transfected Tcells or expanded tumor infiltrating lymphocytes for use in an adoptiveT cell therapy (e.g., in vitro or in a subject), or a chemotherapeuticagent. In some embodiments, the at least one additional agent can beused during the in vitro manufacturing process of an autologous T celltherapy.

In another aspect, this document features an isolated monoclonalantibody that specifically binds to TNFRSF25. The antibody can include(a) a heavy chain containing a CDR1 sequence as set forth in SEQ IDNO:4, a CDR2 sequence as set forth in SEQ ID NO:6, and a CDR3 sequenceas set forth in SEQ ID NO:8, and (b) a light chain containing a CDR1sequence as set forth in SEQ ID NO:11, a CDR2 sequence as set forth inSEQ ID NO:13, and a CDR3 sequence as set forth in SEQ ID NO:15. Theisolated monoclonal antibody can include a heavy chain containing SEQ IDNO:1, 17, 21, 23, or 25, and a light chain comprising SEQ ID NO:2, 26,or 30.

In another aspect, this document features a pharmaceutical compositioncontaining a pharmaceutically acceptable carrier and a human orhumanized monoclonal antibody that specifically binds to TNFRSF25, wherethe antibody comprises includes (a) a heavy chain containing a CDR1sequence as set forth in SEQ ID NO:4, a CDR2 sequence as set forth inSEQ ID NO:6, and a CDR3 sequence as set forth in SEQ ID NO:8, and (b) alight chain containing a CDR1 sequence as set forth in SEQ ID NO:11, aCDR2 sequence as set forth in SEQ ID NO:13, and a CDR3 sequence as setforth in SEQ ID NO:15. In some embodiments, the antibody can include aheavy chain comprising the amino acid sequence set forth in SEQ ID NO:1,17, 21, 23, or 25, and a light chain comprising the amino acid sequenceset forth in SEQ ID NO:2, 26, or 30.

In still another aspect, this document features an isolated monoclonalantibody that binds specifically to TNFRSF25, where the antibodycontains a set of six CDRs that includes no more than four total aminoacid substitutions in the set of six CDRs having the amino acidsequences set forth in SEQ ID NOS:4, 6, 8, 11, 13, and 15. In someembodiments, the set of six CDRs includes no more than two total aminoacid substitutions in the set of six CDRs having the amino acidsequences set forth in SEQ ID NOS:4, 6, 8, 11, 13, and 15.

In another aspect, this document features a pharmaceutical compositioncontaining a pharmaceutically acceptable carrier and a human orhumanized monoclonal antibody that binds specifically to TNFRSF25, wherethe antibody contains a set of six CDRs that includes no more than fourtotal amino acid substitutions in the set of six CDRs having the aminoacid sequences set forth in SEQ ID NOS:4, 6, 8, 11, 13, and 15. In someembodiments, the set of six CDRs includes no more than two total aminoacid substitutions in the set of six CDRs having the amino acidsequences set forth in SEQ ID NOS:4, 6, 8, 11, 13, and 15.

This document also features a method for treating a tumor in a subject.The method can include administering to the subject an amount of acomposition as provided herein that is effective to induce apoptosis ofTNFRSF25-expressing tumor cells in the tumor. The composition caninclude, for example, a pharmaceutically acceptable carrier and a humanor humanized monoclonal antibody that binds specifically to TNFRSF25,where the antibody includes a set of six CDRs that comprises no morethan four total amino acid substitutions in the set of six CDRs havingthe amino acid sequences set forth in SEQ ID NOS:4, 6, 8, 11, 13, and15, or an isolated anti-TNFRSF25 antibody or antigen binding fragmentthereof that includes (i) a heavy chain variable region sequencecontaining the amino acid sequence set forth in SEQ ID NO:1 or the aminoacid sequence of SEQ ID NO:1 with no more than 12 total amino acidsubstitutions, and (ii) a light chain variable region sequencecontaining the amino acid sequence of SEQ ID NO:2 or the amino acidsequence of SEQ ID NO:2 with no more than 11 total amino acidsubstitutions.

In addition, this document features a method for stimulatingproliferation of CD8+ T cells in a subject. The method can includeadministering to the subject a therapeutically effective amount of acomposition as provided herein. Proliferation of CD8+ T cells can beincreased by at least about 20% as compared to the baseline level ofproliferation prior to the administering, as determined by flowcytometry analysis of antigen specific CD8+ T cells.

In yet another aspect, this document features a method for eliciting animmune response in a subject. The method can include administering tothe subject a therapeutically effective amount of a composition asprovided herein.

This document also features a method for stimulating proliferation ofCD4+FoxP3+ regulatory T cells in a subject. The method can includeadministering to the subject a therapeutically effective amount of acomposition as provided herein.

Unless otherwise defined, all technical and scientific terms used hereinhave the same meaning as commonly understood by one of ordinary skill inthe art to which this invention pertains. Although methods and materialssimilar or equivalent to those described herein can be used to practicethe invention, suitable methods and materials are described below. Allpublications, patent applications, patents, and other referencesmentioned herein are incorporated by reference in their entirety. Incase of conflict, the present specification, including definitions, willcontrol. In addition, the materials, methods, and examples areillustrative only and not intended to be limiting.

The details of one or more embodiments of the invention are set forth inthe accompanying drawings and the description below. Other features,objects, and advantages of the invention will be apparent from thedescription and drawings, and from the claims.

DESCRIPTION OF DRAWINGS

FIG. 1 is a graph plotting functional activity of a humanTNFRSF25-specific mAb (PTX-25). P815 cells, or P815 cells expressinghuman TNFRSF25, were exposed in vitro to control human IgG, humanTL1A-Ig, or PTX-25, as indicated. Functional activity of TNFRSF25 wasdetermined by detection of caspase activation in cells expressing humanTNFRSF25 and exposed to a TNFRSF25 agonist (human TL1A-Ig or PTX-25) ascompared to control. Human TL1A-Ig and PTX-25 led to caspase activationin P815 cells expressing human TNFRSF25, but not in P815 cells alone.

FIG. 2 is a graph plotting apoptosis of P815 cells expressing humanTNFRSF25 and treated with the indicated humanized antibodies, asmeasured by caspase 3 activity.

FIG. 3 is a graph plotting binding of PTX-25 to human TNFRSF25-Fc, asdetected using an enzyme linked immunosorbent assay (ELISA).

FIGS. 4A-4B is a scheme for TNFRSF25 antibody humanization.

FIG. 5 is a pair of graphs plotting in vitro stimulation of human CD4+and CD8+ T cell proliferation by PTX-25. Human T cells purified bygradient centrifugation were plated in the presence of plate-boundanti-human CD3 antibody and IL-2, as indicated. PTX-25 was added to theindicated conditions, and proliferation of human CD4+(left panel) andCD8+(right panel) T cells was detected using flow cytometry followingincorporation of Click-Edu reagent in vitro.

FIG. 6 is a graph plotting flow cytometry binding of humanized clones toP815 cells expressing human TNFRSF25.

FIG. 7 is a graph plotting surface plasmon resonance affinity forhumanized antibody clones.

FIG. 8 is a graph plotting functional activity of BMK1, chimericantibody cAb1.hIgG1 (35783), the most potent humanized antibody (hAb2(35816)), and an hTL1A-hFc fusion, as determined by detection of caspaseactivation in vitro.

FIG. 9 is a graph plotting antibody-dependent cell-mediated cytotoxicity(ADCC) for the indicated chimeric and humanized antibodies.

DETAILED DESCRIPTION

This document provides a human TNFRSF25 specific monoclonal antibody(“PTX-25”), as well as humanized versions of the antibody, and antigenbinding fragments of the antibody and its humanized versions. Alsoprovided herein are methods for using PTX-25 to, inter alia, stimulateproliferation of T cells (e.g., human T cells, murine T cells, ormacaque T cells), as well as methods for using PTX-25 in the treatmentof human cancer patients (e.g., by administering an amount of PTX-25that is effective to stimulate proliferation of CD8+ T cells).

As used herein, the term “antibody” refers to any immunoglobulin orantibody (e.g., human, hamster, feline, mouse, cartilaginous fish, orcamelid antibodies), and any derivative or conjugate thereof, thatspecifically binds to an antigen. A wide variety of antibodies are knownby those skilled in the art. Non-limiting examples of antibodies includemonoclonal antibodies, polyclonal antibodies, humanized antibodies,multi-specific antibodies (e.g., bi-specific antibodies), single-chainantibodies (e.g., single-domain antibodies, camelid antibodies, andcartilaginous fish antibodies), chimeric antibodies, feline antibodies,and felinized antibodies. The term antibody also includes antibodyderivatives and conjugates (e.g., an antibody conjugated to astabilizing protein, a detectable moiety, or a therapeutic agent).

By “isolated” or “purified” with respect to a polypeptide (e.g., anantibody or a fragment thereof), it is meant that the polypeptide isseparated to some extent from the cellular components with which wouldnormally be found in nature (e.g., other polypeptides, lipids,carbohydrates, and nucleic acids). In some embodiments, an “isolated”polypeptide is one that is expressed and produced in an environmentother than the environment in which the polypeptide would naturallyexpressed and produced. For example, a plant polypeptide is isolatedwhen expressed and produced in bacteria or fungi. Similarly, a plantpolypeptide is isolated when its gene coding sequence is operably linkedto a chimeric regulatory element and expressed in a tissue where thepolypeptide is not naturally expressed.

An isolated polypeptide can yield a single major band on a non-reducingpolyacrylamide gel. An isolated polypeptide can be at least about 75%pure (e.g., at least 80%, 85%, 90%, 95%, 97%, 98%, 99%, or 100% pure).Isolated polypeptides can be obtained by, for example, extraction from anatural source, by chemical synthesis, or by recombinant production in ahost cell or transgenic plant, and can be purified using, for example,affinity chromatography, immunoprecipitation, size exclusionchromatography, and ion exchange chromatography. The extent ofpurification can be measured using any appropriate method, including,without limitation, column chromatography, polyacrylamide gelelectrophoresis, or high-performance liquid chromatography.

An “antigen binding fragment” is any portion of a full-length antibodythat contains at least one variable domain (e.g., a variable domain of amammalian (e.g., feline, human, hamster, or mouse) heavy or light chainimmunoglobulin, a camelid variable antigen binding domain (VHH), or acartilaginous fish immunoglobulin new antigen receptor (Ig-NAR) domain)that is capable of specifically binding to an antigen. Non-limitingexamples of antibody fragments include Fab, Fab′, F(ab′)2, and Fvfragments, diabodies, linear antibodies, and multi-specific antibodiesformed from antibody fragments. Additional antibody fragments containingat least one camelid VHH domain or at least one cartilaginous fishIg-NAR domain include mini-bodies, micro-antibodies, subnano-antibodies,and nano-antibodies, and any of the other forms of antibodies described,for example, in U.S. Publication No. 2010/0092470.

An “Fv fragment” is the minimum antibody fragment that contains acomplete antigen recognition and binding site. This region consists of adimer of one heavy chain variable domain and one light chain variabledomain in tight, non-covalent association. It is in this configurationthat the three complementary determining regions (CDRs) of each variabledomain interact to define an antigen binding site on the surface of theVH-VL dimer. As used herein, the term “complementary determining region”or “CDR” refers to a region within an immunoglobulin (a heavy or lightchain immunoglobulin) that forms part of an antigen binding site in anantibody or antigen binding fragment thereof. As is known in the art,heavy chain and light chain immunoglobulins each contain three CDRs,referred to as CDR1, CDR2, and CDR3. In any antibody or antigen bindingfragment, the three CDRs from the heavy chain immunoglobulin and thethree CDRs from the light chain immunoglobulin together form an antigenbinding site in the antibody or antigen binding fragment thereof. TheKabat Database is one system used in the art to number CDR sequencespresent in a light chain immunoglobulin or a heavy chain immunoglobulin.

Collectively, the six CDR's confer antigen binding specificity to theantibody. However, even a single variable domain (or half of an Fvcomprising only three CDR's specific for an antigen) has the ability torecognize and bind the antigen, although usually at a lower affinitythan the entire binding site. The “Fab fragment” also contains theconstant domain of the light chain and the first constant domain (CHI)of the heavy chain. The “Fab fragment” differs from the “Fab′ fragment”by the addition of a few residues at the carboxy terminus of the heavychain CHI domain, including one or more cysteines from the antibodyhinge region. The “F(ab′)2 fragment” originally is produced as a pair of“Fab′ fragments” which have hinge cysteines between them. Methods ofpreparing such antibody fragments, such as papain or pepsin digestion,are known to those skilled in the art.

An antibody can be of the IgA-, IgD-, IgE, IgG- or IgM-type, includingIgG- or IgM-types such as, without limitation, IgG1-, IgG2-, IgG3-,IgG4-, IgM1- and IgM2-types. For example, in some cases, the antibody isof the IgG1-, IgG2- or IgG4-type.

In some embodiments, antibodies as provided herein can be fully human orhumanized antibodies. By “human antibody” is meant an antibody that isencoded by a nucleic acid (e.g., a rearranged human immunoglobulin heavyor light chain locus) present in the genome of a human. In someembodiments, a human antibody can be produced in a human cell culture(e.g., feline hybridoma cells). In some embodiments, a human antibodycan be produced in a non-human cell (e.g., a mouse or hamster cellline). In some embodiments, a human antibody can be produced in abacterial or yeast cell.

Human antibodies can avoid certain problems associated with xenogeneicantibodies, such as antibodies that possess murine or rat variableand/or constant regions. For example, because the effector portion ishuman, it can interact better with other parts of the human immunesystem, e.g., to destroy target cells more efficiently bycomplement-dependent cytotoxicity or antibody-dependent cellularcytotoxicity. In addition, the human immune system should not recognizethe antibody as foreign. Further, half-life in human circulation will besimilar to naturally occurring human antibodies, allowing smaller andless frequent doses to be given. Methods for preparing human antibodiesare known in the art.

As used herein, the term “humanized antibody” refers to a human antibodythat contains minimal sequence derived from non-human (e.g., mouse,hamster, rat, rabbit, or goat) immunoglobulin. Humanized antibodiesgenerally are chimeric or mutant monoclonal antibodies from mouse, rat,hamster, rabbit or other species, bearing human constant and/or variableregion domains or specific changes. In non-limiting examples, humanizedantibodies are human antibodies (recipient antibody) in whichhypervariable region (HVR) residues of the recipient antibody arereplaced by HVR residues from a non-human species (donor) antibody, suchas a mouse, rat, rabbit, or goat antibody having the desiredspecificity, affinity, and capacity. In some embodiments, Fv frameworkresidues of the human immunoglobulin can be replaced by correspondingnon-human residues. In some embodiments, humanized antibodies cancontain residues that are not found in the recipient antibody or in thedonor antibody. Such modifications can be made to refine antibodyperformance, for example.

In some embodiments, a humanized antibody can contain substantially allof at least one, and typically two, variable domains, in which all orsubstantially all of the hypervariable loops (CDRs) correspond to thoseof a non-human immunoglobulin, while all or substantially all of theframework regions are those of a human immunoglobulin sequence. Ahumanized antibody also can contain at least a portion of animmunoglobulin constant (Fc) region, typically that of a humanimmunoglobulin.

In some embodiments, humanized antibody or antigen binding fragment asprovided herein can have reduced or minimal effector function (e.g., ascompared to corresponding, non-humanized antibody), such that it doesnot stimulate effector cell action to the same extent that acorresponding non-humanized antibody would.

Techniques for generating humanized antibodies are well known to thoseof skill in the art. In some embodiments, controlled rearrangement ofantibody domains joined through protein disulfide bonds to form new,artificial protein molecules or “chimeric” antibodies can be utilized(Konieczny et al., Haematologia (Budap.) 14:95, 1981). Recombinant DNAtechnology can be used to construct gene fusions between DNA sequencesencoding mouse antibody variable light and heavy chain domains and humanantibody light and heavy chain constant domains (Morrison et al., ProcNatl Acad Sci USA 81:6851, 1984). For example, DNA sequences encodingantigen binding portions or CDRs of murine monoclonal antibodies can begrafted by molecular means into DNA sequences encoding frameworks ofhuman antibody heavy and light chains (Jones et al., Nature 321:522,1986; and Riechmann et al., Nature 332:323, 1988). Expressed recombinantproducts are called “reshaped” or humanized antibodies, and contain theframework of a human antibody light or heavy chain and antigenrecognition portions, CDRs, of a murine monoclonal antibody.

Other methods for designing heavy and light chains and for producinghumanized antibodies are described in, for example, U.S. Pat. Nos.5,530,101; 5,565,332; 5,585,089; 5,639,641; 5,693,761; 5,693,762; and5,733,743. Yet additional methods for humanizing antibodies aredescribed in U.S. Pat. Nos. 4,816,567; 4,935,496; 5,502,167; 5,558,864;5,693,493; 5,698,417; 5,705,154; 5,750,078; and 5,770,403, for example.

The term “single-chain antibody” refers to a single polypeptide thatcontains at least one variable binding domain (e.g., a variable domainof a mammalian heavy or light chain immunoglobulin, a camelid VHH, or acartilaginous fish (e.g., shark) Ig-NAR domain) that is capable ofspecifically binding to an antigen. Non-limiting examples ofsingle-chain antibodies include single-domain antibodies.

As used herein, the term “single-domain antibody” refers to apolypeptide that contains one camelid VHH or at least one cartilaginousfish Ig-NAR domain that is capable of specifically binding to anantigen. Non-limiting examples of single-domain antibodies aredescribed, for example, in U.S. Publication No. 2010/0092470.

An antibody or antigen binding fragment thereof “specifically binds” toa particular antigen, e.g., TNFRFS25, when it binds to that antigen in asample, and does not recognize and bind, or recognizes and binds to alesser extent, other molecules in the sample. In some embodiments, anantibody or an antigen binding fragment thereof can selectively bind toan epitope with an affinity (K_(D)) equal to or less than, for example,about 1×10⁻⁶ M (e.g., equal to or less than about 1×10⁻⁹ M, equal to orless than about 1×10⁻¹⁰ M, equal to or less than about 1×10⁻¹¹ M, orequal to or less than about 1×10⁻¹² M) in phosphate buffered saline. Theability of an antibody or antigen binding fragment to specifically binda protein epitope can be determined using any of the methods known inthe art or those methods described herein. This can include, forexample, binding to TNFRSF25 on live cells as a method to stimulatecaspase activation in live transformed cells (FIG. 2 and TABLE 1),binding to an immobilized target substrate including human TNFRSF25fusion proteins as detected using an ELISA method (FIG. 3), binding toTNFRSF25 on live cells as detected by flow cytometry (FIG. 6 and TABLE2), or binding to an immobilized substrate by surface plasmon resonance(including ProteOn) (FIG. 7 and TABLE 3).

As described herein, a monoclonal antibody against TNFRSF25 wasisolated, and the amino acid sequences of the variable heavy and lightchains were determined to contain SEQ ID NOS:1 and 2, respectively. Asdescribed in Example 4 below, the antibody was humanized, such thatseveral humanized VH (SEQ ID NOS:17, 21, 23, and 25) and VL (SEQ IDNOS:26 and 30) genes were designed using homologous frameworks of humangerm line genes (FIGS. 4A-B).

Thus, this document provides heavy chain variable region polypeptidescontaining the amino acid sequence set forth in SEQ ID NO:1, 17, 21, 23,or 25, or an antigen binding fragment thereof, as well as polypeptideshaving at least about 90% (e.g., about 91%, about 92%, about 93%, about94%, about 95%, about 96%, about 97%, about 98%, or about 99%) aminoacid sequence identity to SEQ ID NO:1, 17, 21, 23, or 25, or an antigenbinding fragment thereof. In some embodiments, a heavy chain variableregion polypeptide can contain 12 or less (e.g., 12, 11, ten, nine,eight, seven, six, five, four, three, two, or one) amino acidsubstitution as compared to SEQ ID NO:1, 17, 21, 23, or 25, or anantigen binding fragment thereof.

In some embodiments, a heavy chain variable region polypeptide caninclude the CDR1 sequence set forth in SEQ ID NO:4, the CDR2 sequenceset forth in SEQ ID NO:6, and the CDR3 sequence set forth in SEQ IDNO:8. The polypeptide also can include variable region heavy chainframework (FW) sequences juxtaposed between the CDRs, according to theformula (FW1)-(CDR1)-(FW2)-(CDR2)-(FW3)-(CDR3)-(FW4), for example. Insome embodiments, the FW sequences can be human sequences. In someembodiments, a heavy chain variable region polypeptide can include theFW1 sequence set forth in SEQ ID NO:3, SEQ ID NO:18, or SEQ ID NO:22,the FW2 sequence set forth in SEQ ID NO:5, SEQ ID NO:19, or SEQ IDNO:24, the FW3 sequence set forth in SEQ ID NO:7 or SEQ ID NO:20, andthe FW4 sequence set forth in SEQ ID NO:9. Particular combinations ofheavy chain variable region CDR and FW sequences are set forth in theExamples herein. It is to be noted, however, that this documentcontemplates other combinations of the disclosed CDR and FW sequences.

This document also provides light chain variable region polypeptidescontaining the amino acid sequence set forth in SEQ ID NO:2, 26, or 30,or an antigen binding fragment thereof, as well as polypeptides havingat least about 90% (e.g., about 91%, about 92%, about 93%, about 94%,about 95%, about 96%, about 97%, about 98%, or about 99%) amino acidsequence identity to SEQ ID NO:2, 26, or 30, or an antigen bindingfragment thereof. In some embodiments, a light chain variable regionpolypeptide can contain 11 or less (e.g., 11, ten, nine, eight, seven,six, five, four, three, two, or one) amino acid substitutions ascompared to SEQ ID NO:2, 26, or 30, or an antigen binding fragmentthereof.

In some embodiments, a light chain variable region polypeptide cancontain the CDR1 sequence set forth in SEQ ID NO:11, the CDR2 sequenceset forth in SEQ ID NO:13, and the CDR3 sequence set forth in SEQ IDNO:15. The polypeptide also can include variable region light chain FWjuxtaposed between the CDRs, according to the formula(FW1)-(CDR1)-(FW2)-(CDR2)-(FW3)-(CDR3)-(FW4). In some cases, the FWsequences can be human sequences. In some embodiments, a light chainvariable region polypeptide can include the FW1 sequence set forth inSEQ ID NO:10, SEQ ID NO:27, or SEQ ID NO:31, the FW2 sequence set forthin SEQ ID NO:12, SEQ ID NO:28, or SEQ ID NO:32, the FW3 sequence setforth in SEQ ID NO:14, SEQ ID NO:29, or SEQ ID NO:33, and the FW4sequence set forth in SEQ ID NO:16. Particular combinations of lightchain variable region CDR and FW sequences are set forth in the Examplesherein. It is to be noted, however, that this document contemplatesother combinations of the disclosed CDR and FW sequences.

This document also provides antibodies and antigen binding fragmentsthat contain both a heavy chain variable region polypeptide and a lightchain variable region polypeptide as disclosed herein. In someembodiments, for example, an antibody or antigen binding fragment cancontain both a heavy chain variable region sequence comprising the aminoacid sequence set forth in SEQ ID NO:1, or the amino acid sequence ofSEQ ID NO:1 with no more than 12 total amino acid substitutions (e.g.,no more than ten, no more than eight, no more than six, no more thanfour, or no more than two total amino acid substitutions), and a lightchain variable region sequence comprising the amino acid sequence of SEQID NO:2, or the amino acid sequence of SEQ ID NO:2 with no more than 11total amino acid substitutions (e.g., no more than nine, no more thanseven, no more than five, no more than three, or no more than one totalamino acid substitution). An amino acid substitution refers to thereplacement of one amino acid residue with another in a peptidesequence.

In some embodiments, amino acid substitutions can be made by selectingconservative substitutions that do not differ significantly in theireffect on maintaining (a) the structure of the peptide backbone in thearea of the substitution, (b) the charge or hydrophobicity of themolecule at the target site, or (c) the bulk of the side chain. Forexample, naturally occurring residues can be divided into groups basedon side-chain properties: (1) hydrophobic amino acids (norleucine,methionine, alanine, valine, leucine, and isoleucine); (2) neutralhydrophilic amino acids (cysteine, serine, and threonine); (3) acidicamino acids (aspartic acid and glutamic acid); (4) basic amino acids(asparagine, glutamine, histidine, lysine, and arginine); (5) aminoacids that influence chain orientation (glycine and proline); and (6)aromatic amino acids (tryptophan, tyrosine, and phenylalanine).Substitutions made within these groups can be considered conservativesubstitutions. Non-limiting examples of conservative substitutionsinclude, without limitation, substitution of valine for alanine, lysinefor arginine, glutamine for asparagine, glutamic acid for aspartic acid,serine for cysteine, asparagine for glutamine, aspartic acid forglutamic acid, proline for glycine, arginine for histidine, leucine forisoleucine, isoleucine for leucine, arginine for lysine, leucine formethionine, leucine for phenyalanine, glycine for proline, threonine forserine, serine for threonine, tyrosine for tryptophan, phenylalanine fortyrosine, and/or leucine for valine. In some embodiments, an amino acidsubstitution can be non-conservative, such that a member of one of theamino acid classes described above is exchanged for a member of anotherclass.

The percent sequence identity between a particular nucleic acid or aminoacid sequence and a sequence referenced by a particular sequenceidentification number is determined as follows. First, a nucleic acid oramino acid sequence is compared to the sequence set forth in aparticular sequence identification number using the BLAST 2 Sequences(B12seq) program from the stand-alone version of BLASTZ containingBLASTN version 2.0.14 and BLASTP version 2.0.14. This stand-aloneversion of BLASTZ can be obtained online at fr.com/blast or atncbi.nlm.nih.gov. Instructions explaining how to use the B12seq programcan be found in the readme file accompanying BLASTZ. B12seq performs acomparison between two sequences using either the BLASTN or BLASTPalgorithm. BLASTN is used to compare nucleic acid sequences, whileBLASTP is used to compare amino acid sequences. To compare two nucleicacid sequences, the options are set as follows: -i is set to a filecontaining the first nucleic acid sequence to be compared (e.g.,C:\seq1.txt); -j is set to a file containing the second nucleic acidsequence to be compared (e.g., C:\seq2.txt); -p is set to blastn; -o isset to any desired file name (e.g., C:\output.txt); -q is set to −1; -ris set to 2; and all other options are left at their default setting.For example, the following command can be used to generate an outputfile containing a comparison between two sequences: C:\Bl2seq -ic:\seq1.txt -j c:\seq2.txt -p blastn -o c:\output.txt -q −1 -r 2. Tocompare two amino acid sequences, the options of B12seq are set asfollows: -i is set to a file containing the first amino acid sequence tobe compared (e.g., C:\seq1.txt); -j is set to a file containing thesecond amino acid sequence to be compared (e.g., C:\seq2.txt); -p is setto blastp; -o is set to any desired file name (e.g., C:\output.txt); andall other options are left at their default setting. For example, thefollowing command can be used to generate an output file containing acomparison between two amino acid sequences: C:Bl2seq -i c:\seq1.txt -jc:\seq2.txt -p blastp -o c:\output.txt. If the two compared sequencesshare homology, then the designated output file will present thoseregions of homology as aligned sequences. If the two compared sequencesdo not share homology, then the designated output file will not presentaligned sequences.

Once aligned, the number of matches is determined by counting the numberof positions where an identical nucleotide or amino acid residue ispresented in both sequences. The percent sequence identity is determinedby dividing the number of matches either by the length of the sequenceset forth in the identified sequence (e.g., SEQ ID NO:1), or by anarticulated length (e.g., 100 consecutive nucleotides or amino acidresidues from a sequence set forth in an identified sequence), followedby multiplying the resulting value by 100. For example, an amino acidsequence that has 110 matches when aligned with the sequence set forthin SEQ ID NO:1 is 90.9 percent identical to the sequence set forth inSEQ ID NO:1 (i.e., 110÷121×100=90.9). It is noted that the percentsequence identity value is rounded to the nearest tenth. For example,75.11, 75.12, 75.13, and 75.14 is rounded down to 75.1, while 75.15,75.16, 75.17, 75.18, and 75.19 is rounded up to 75.2. It also is notedthat the length value will always be an integer.

This document also provides pharmaceutical compositions that contain anantibody or antigen binding fragment as described herein, in combinationwith a pharmaceutically acceptable carrier. A “pharmaceuticallyacceptable carrier” (also referred to as an “excipient” or a “carrier”)is a pharmaceutically acceptable solvent, suspending agent, stabilizingagent, or any other pharmacologically inert vehicle for delivering oneor more therapeutic compounds to a subject (e.g., a mammal, such as ahuman, non-human primate, dog, cat, sheep, pig, horse, cow, mouse, rat,or rabbit), which is nontoxic to the cell or subject being exposedthereto at the dosages and concentrations employed. Pharmaceuticallyacceptable carriers can be liquid or solid, and can be selected with theplanned manner of administration in mind so as to provide for thedesired bulk, consistency, and other pertinent transport and chemicalproperties, when combined with one or more of therapeutic compounds andany other components of a given pharmaceutical composition. Typicalpharmaceutically acceptable carriers that do not deleteriously reactwith amino acids include, by way of example and not limitation: water,saline solution, binding agents (e.g., polyvinylpyrrolidone orhydroxypropyl methylcellulose), fillers (e.g., lactose and other sugars,gelatin, or calcium sulfate), lubricants (e.g., starch, polyethyleneglycol, or sodium acetate), disintegrates (e.g., starch or sodium starchglycolate), and wetting agents (e.g., sodium lauryl sulfate).Pharmaceutically acceptable carriers also include aqueous pH bufferedsolutions or liposomes (small vesicles composed of various types oflipids, phospholipids and/or surfactants which are useful for deliveryof a drug to a mammal). Further examples of pharmaceutically acceptablecarriers include buffers such as phosphate, citrate, and other organicacids, antioxidants such as ascorbic acid, low molecular weight (lessthan about 10 residues) polypeptides, proteins such as serum albumin,gelatin, or immunoglobulins, hydrophilic polymers such aspolyvinylpyrrolidone, amino acids such as glycine, glutamine,asparagine, arginine or lysine, monosaccharides, disaccharides, andother carbohydrates including glucose, mannose or dextrins, chelatingagents such as EDTA, sugar alcohols such as mannitol or sorbitol,salt-forming counterions such as sodium, and/or nonionic surfactantssuch as TWEEN™, polyethylene glycol (PEG), and PLURONICS™.

Pharmaceutical compositions can be formulated by mixing one or moreactive agents with one or more physiologically acceptable carriers,diluents, and/or adjuvants, and optionally other agents that are usuallyincorporated into formulations to provide improved transfer, delivery,tolerance, and the like. A pharmaceutical composition can be formulated,e.g., in lyophilized formulations, aqueous solutions, dispersions, orsolid preparations, such as tablets, dragees or capsules. A multitude ofappropriate formulations can be found in the formulary known to allpharmaceutical chemists: Remington's Pharmaceutical Sciences (18th ed,Mack Publishing Company, Easton, Pa. (1990)), particularly Chapter 87 byBlock, Lawrence, therein. These formulations include, for example,powders, pastes, ointments, jellies, waxes, oils, lipids, lipid(cationic or anionic) containing vesicles (such as LIPOFECTIN™), DNAconjugates, anhydrous absorption pastes, oil-in-water and water-in-oilemulsions, emulsions carbowax (polyethylene glycols of various molecularweights), semi-solid gels, and semi-solid mixtures containing carbowax.Any of the foregoing mixtures may be appropriate in treatments andtherapies as described herein, provided that the active agent in theformulation is not inactivated by the formulation and the formulation isphysiologically compatible and tolerable with the route ofadministration. See, also, Baldrick, Regul Toxicol Pharmacol 32:210-218,2000; Wang, Int J Pharm 203:1-60, 2000; Charman J Pharm Sci 89:967-978,2000; and Powell et al. PDA J Pharm Sci Technol 52:238-311, 1998), andthe citations therein for additional information related toformulations, excipients and carriers well known to pharmaceuticalchemists.

Pharmaceutical compositions include, without limitation, solutions,emulsions, aqueous suspensions, and liposome-containing formulations.These compositions can be generated from a variety of components thatinclude, for example, preformed liquids, self-emulsifying solids andself-emulsifying semisolids. Emulsions are often biphasic systemscomprising of two immiscible liquid phases intimately mixed anddispersed with each other; in general, emulsions are either of thewater-in-oil (w/o) or oil-in-water (o/w) variety. Emulsion formulationshave been widely used for oral delivery of therapeutics due to theirease of formulation and efficacy of solubilization, absorption, andbioavailability.

Compositions and formulations can contain sterile aqueous solutions,which also can contain buffers, diluents and other suitable additives(e.g., penetration enhancers, carrier compounds and otherpharmaceutically acceptable carriers). Compositions additionally cancontain other adjunct components conventionally found in pharmaceuticalcompositions. Thus, the compositions also can include compatible,pharmaceutically active materials such as, for example, antipruritics,astringents, local anesthetics or anti-inflammatory agents, oradditional materials useful in physically formulating various dosageforms of the compositions provided herein, such as dyes, flavoringagents, preservatives, antioxidants, opacifiers, thickening agents andstabilizers. Furthermore, the composition can be mixed with auxiliaryagents, e.g., lubricants, preservatives, stabilizers, wetting agents,emulsifiers, salts for influencing osmotic pressure, buffers, colorings,flavorings, and aromatic substances. When added, however, such materialsshould not unduly interfere with the biological activities of thepolypeptide components within the compositions provided herein. Theformulations can be sterilized if desired.

In some embodiments, a composition containing an antibody or antigenbinding fragment as provided herein (e.g., PTX-25 or an antigen bindingfragment thereof) can be in the form of a solution or powder with orwithout a diluent to make an injectable suspension. The composition maycontain additional ingredients including, without limitation,pharmaceutically acceptable vehicles, such as saline, water, lacticacid, mannitol, or combinations thereof, for example.

Any appropriate method can be used to administer an antibody or antigenbinding fragment as described herein to a mammal. Administration can be,for example, parenteral (e.g., by subcutaneous, intrathecal,intraventricular, intramuscular, or intraperitoneal injection, or byintravenous drip). Administration can be rapid (e.g., by injection) orcan occur over a period of time (e.g., by slow infusion oradministration of slow release formulations). In some embodiments,administration can be topical (e.g., transdermal, sublingual,ophthalmic, or intranasal), pulmonary (e.g., by inhalation orinsufflation of powders or aerosols), or oral. In addition, acomposition containing an antibody or antigen binding fragment asdescribed herein can be administered prior to, after, or in lieu ofsurgical resection of a tumor.

A composition containing an anti-TNFRSF25 antibody or antigen bindingfragment can be administered to a mammal in any appropriate amount, atany appropriate frequency, and for any appropriate duration effective toachieve a desired outcome. For example, an anti-TNFRSF25 antibody orantigen binding fragment can be administered to a subject in an amounteffective to stimulate proliferation of T cells in vitro or in vivo(e.g., human, murine, hamster, or macaque T cells, including CD8+ Tcells and/or CD4+FoxP3+ regulatory T cells), to stimulate apoptosis oftumor cells that express TNFRSF25, to reduce tumor size, or to increaseprogression-free survival of a cancer patient.

Administration to a subject of an antibody or antigen binding fragmentas provided herein can result in increased numbers of T cells (e.g.,naturally-occurring tumor-reactive CD8+ T cells or CD4+FoxP3+ regulatoryT cells) that can exert anti-cancer effects against cancer cells presentwithin the mammal. Thus, this document also provides methods forstimulating proliferation of T cells in a subject, by administering tothe subject an antibody, antigen-binding fragment, or composition asdisclosed herein. In some cases, a composition containing ananti-TNFRSF25 antibody or antigen binding fragment as described hereincan be administered to a subject in an amount effective to increaseproliferation of T cells (e.g., by at least about 10 percent, about 20percent, about 25 percent, about 50 percent, about 60 percent, about 70percent, about 75 percent, about 80 percent, about 90 percent, about 100percent, or more than 100 percent), as compared to the “baseline” levelof T cell proliferation in the subject prior to administration of thecomposition, or as compared to the level of T cell proliferation in acontrol subject or population of subjects to whom the composition wasnot administered. The T cells can be, for example, CD8+ T cells, orCD4+FoxP3+ regulatory T cells. Any suitable method can be used todetermine whether or not the level of T cell proliferation is increasedin the subject. Such methods can include, without limitation, flowcytometry analysis of antigen specific T cells (e.g., flow cytometryanalysis of the proportion of antigen specific CD8+ T cells as afraction of the total CD8+ T cell pool), analysis of cell proliferationmarkers (e.g., expression of Ki67) in CD8+ T cells, increased counts ofCD8+ T cells, or increased proportions of individual TCR sequences of aparticular clone of CD8+ T cells.

This document also provides methods for promoting apoptosis ofTNFRSF25-expressing tumor cells in a subject, by treating the subjectwith an antibody, antigen-binding fragment, or composition as describedherein. In some cases, a composition containing an antibody or antigenbinding fragment as provided herein can be administered to a subject(e.g., a cancer patient) in an amount effective to increase apoptosis ofTNFRSF25-expressing tumor cells (e.g., by at least about 10 percent,about 20 percent, about 25 percent, about 50 percent, about 60 percent,about 70 percent, about 75 percent, about 80 percent, about 90 percent,about 100 percent, or more than 100 percent), as compared to the“baseline” level of tumor cell apoptosis in the subject prior toadministration of the composition, or as compared to the level of tumorcell apoptosis in a control subject or population of subjects to whomthe composition was not administered. Any suitable method can be used todetermine whether or not the level of tumor cell apoptosis is increasedin the subject. This can include, for example, radiologic techniquessuch as CT or MRI, with or without contrast that indicates the presenceof a necrotic or apoptotic tumor, biopsy of a tumor sample indicatingincreased tumor cell death, caspase induction within tumor cells,elimination of detectable tumor lesions by radiologic, or surgical orphysical examination.

Methods for treating a subject (e.g., a human patient) with cancer alsoare provided herein. In some cases, a composition containing an antibodyor antigen binding fragment as described herein can be administered to asubject having cancer in an amount effective to reduce the progressionrate of the cancer (e.g., by at least about 10 percent, about 20percent, about 25 percent, about 50 percent, about 60 percent, about 70percent, about 75 percent, about 80 percent, about 90 percent, or morethan 90 percent), as compared to the rate of cancer progression in thesubject prior to administration of the composition, or as compared tothe rate of cancer progression in a control subject or population ofsubjects to whom the composition was not administered. In someembodiments, the progression rate can be reduced such that no additionalcancer progression is detected. Any appropriate method can be used todetermine whether or not the progression rate of cancer is reduced. Forskin cancer (e.g., melanoma), for example, the progression rate can beassessed by imaging tissue at different time points and determining theamount of cancer cells present. The amounts of cancer cells determinedwithin tissue at different times can be compared to determine theprogression rate. After treatment as described herein, the progressionrate can be determined again over another time interval. In some cases,the stage of cancer after treatment can be determined and compared tothe stage before treatment to determine whether or not the progressionrate has been reduced.

A composition containing an antibody or antigen binding fragment asdescribed herein also can be administered to a subject having cancerunder conditions where progression-free survival is increased (e.g., byat least about 10 percent, about 20 percent, about 25 percent, about 50percent, about 60 percent, about 70 percent, about 75 percent, about 80percent, about 90 percent, about 100 percent, or more than 100 percent),as compared to the median progression-free survival of correspondingsubjects having untreated cancer or the median progression-free survivalof corresponding subjects having cancer and treated with other therapies(e.g., chemotherapeutic agents alone). Progression-free survival can bemeasured over any length of time (e.g., one month, two months, threemonths, four months, five months, six months, or longer).

An effective amount of a composition containing a molecule as providedherein can be any amount that has a desired defect (e.g., stimulatesproliferation of CD8+ T cells, stimulates apoptosis ofTNFRSF25-expressing tumor cells, stimulates or elicits an immuneresponse in a subject, reduces tumor size, reduces the progression rateof cancer, increases progression-free survival of a cancer patient, orincreases the median time to progression without producing significanttoxicity). Optimum dosages can vary depending on the relative potency ofindividual polypeptides (e.g., antibodies and antigen bindingfragments), and can generally be estimated based on EC₅₀ found to beeffective in in vitro and in vivo animal models. Typically, dosage isfrom 0.01 μg to 100 g per kg of body weight. For example, an effectiveamount of an antibody or antigen binding fragment can be from about 0.1mg/kg to about 50 mg/kg (e.g., about 0.4 mg/kg, about 2 mg/kg, about 5mg/kg, about 10 mg/kg, about 20 mg/kg, about 30 mg/kg, about 40 mg/kg,or about 50 mg/kg), or any range there between, such as about 0.1 mg/kgto about 10 mg/kg, about 0.4 mg/kg to about 20 mg/kg, about 2 mg/kg toabout 30 mg/kg, or about 5 mg/kg to about 40 mg/kg. If a particularsubject fails to respond to a particular amount, then the amount of theantibody or antigen binding fragment can be increased by, for example,two fold. After receiving this higher concentration, the subject can bemonitored for both responsiveness to the treatment and toxicitysymptoms, and adjustments made accordingly. The effective amount canremain constant or can be adjusted as a sliding scale or variable dosedepending on the subject's response to treatment. Various factors caninfluence the actual effective amount used for a particular application.For example, the frequency of administration, duration of treatment, useof multiple treatment agents, route of administration, and severity ofthe cancer may require an increase or decrease in the actual effectiveamount administered.

The frequency of administration can be any frequency that, for example,stimulates proliferation of CD8+ T cells, stimulates apoptosis ofTNFRSF25-expressing tumor cells, reduces tumor size, reduces theprogression rate of cancer, increases progression-free survival of acancer patient, or increases the median time to progression withoutproducing significant toxicity. For example, the frequency ofadministration can be once or more daily, biweekly, weekly, monthly, oreven less. The frequency of administration can remain constant or can bevariable during the duration of treatment. A course of treatment caninclude rest periods. For example, a composition containing an antibodyor antigen binding fragment as provided herein can be administered overa two week period followed by a two week rest period, and such a regimencan be repeated multiple times. As with the effective amount, variousfactors can influence the actual frequency of administration used for aparticular application. For example, the effective amount, duration oftreatment, use of multiple treatment agents, route of administration,and severity of the cancer may require an increase or decrease inadministration frequency.

An effective duration for administering a composition provided hereincan be any duration that stimulates proliferation of CD8+ T cells,stimulates apoptosis of TNFRSF25-expressing tumor cells, reduces tumorsize, reduces the progression rate of cancer, increases progression-freesurvival of a cancer patient, or increases the median time toprogression without producing significant toxicity. Thus, an effectiveduration can vary from several days to several weeks, months, or years.In general, the effective duration for the treatment of cancer can rangein duration from several weeks to several months. In some cases, aneffective duration can be for as long as an individual subject is alive.Multiple factors can influence the actual effective duration used for aparticular treatment. For example, an effective duration can vary withthe frequency of administration, effective amount, use of multipletreatment agents, route of administration, and severity of the cancer.

After administering a composition as provided herein to a cancerpatient, the patient can be monitored to determine whether or not thecancer was treated. For example, a subject can be assessed aftertreatment to determine whether or not the progression rate of the cancerhas been reduced (e.g., stopped). Any method, including those that arestandard in the art, can be used to assess progression and survivalrates.

A method for using an antibody or antigen binding fragment as providedherein can be combined with known methods of treatment for cancer, forexample, either as combined or additional treatment steps, or asadditional components of a therapeutic formulation. For example,enhancing a host's immune function can be useful to combat tumors.Methods can include, without limitation, APC enhancement, such as byinjection into a tumor of DNA encoding foreign MHC antigens (includingtumor antigens, mutation derived antigens, or other antigens), ortransfecting biopsied tumor cells with genes that increase theprobability of immune antigen recognition (e.g., immune stimulatorycytokines, GM-CSF, or co-stimulatory molecules B7.1, B7.2) of the tumor.Other methods can include, for example, solubilization of specific tumorantigens into depot or sustained release preparations, transfection ofallogeneic tumor cells with adjuvant proteins or antigen carrierproteins, transfection of allogeneic tumor cells with immune stimulatoryproteins such as alpha galactosylceramide, incorporation of specifictumor antigens into virus-derived vaccine regimens, incorporation ofspecific tumor antigens into Listeria derived vaccine regimens, adoptivecellular immunotherapy (including chimeric antigen receptor transfectedT cells), or treatment with activated tumor-specific T-cells (includingex vivo expanded tumor infiltrating lymphocytes). Adoptive cellularimmunotherapy can include isolating tumor-infiltrating hostT-lymphocytes and expanding the population in vitro (e.g., bystimulation with IL-2). The T-cells then can be re-administered to thehost. Other treatments that can be used in combination with an antibodyor antigen-binding fragment as provided herein include, for example,radiation therapy, chemotherapy, hormonal therapy, and the use ofangiogenesis inhibitors.

Thus, in some embodiments, an anti-TNFRSF25 antibody or antigen bindingfragment can be used in combination with one or more additionalmonoclonal antibodies that inhibit binding of PD-L1 to PD-1, inhibitbinding of CTLA-4 to CD80 or CD86, or activate signaling via theTNFRSF4, TNFRSF9, or TNFRSF18 pathways, for example. This also caninclude administration with another antibody, fusion protein, or smallmolecule that binds a specific target on a tumor cell (e.g.,combinations with monoclonal antibodies that bind targets such as CD20,Her2, EGFRvIII, DR4, DR5, VEGF, CD39, and CD73). An anti-TNFRSF25antibody or antigen binding fragment also can be used in combinationwith a cancer vaccine approach to enhance the activation of tumorantigen specific T cells in a cancer patient. In addition, ananti-TNFRSF25 antibody or antigen binding fragment can be used afteradministration of autologous or allogeneic T or NK cells engineered toexpress a chimeric T cell receptor that recognizes a specific tumorantigen. Further, an anti-TNFRSF25 antibody or antigen binding fragmentcan be used in combination with specific chemotherapy or radiationtherapy strategies as a method to expand tumor specific T cells andenhance the activity of either approach as a monotherapy in a cancerpatient.

When one or more conventional therapies are combined with treatmentusing an anti-TNFRSF25 antibody or antigen binding fragment as providedherein for treating cancer, for example, the conventional therapy(ies)can be administered prior to, subsequent to, or simultaneously withadministration of the anti-TNFRSF25 antibody or antigen bindingfragment. For example, a PD-1 blocking antibody can be administered to apatient prior to administration of a TNFRSF25 agonist antibody. Such aregimen can be cycled over a period of weeks, months, or years, forexample. Alternatively, a PD-1 blocking antibody can be administered atthe same time or after administration of a TNFRSF25 agonist antibody.Such a regimen also can be cycled over a period of weeks, months, oryears. In some embodiments, combination therapies that are repeatedlyadministered over a period of time can include two or more of the aboveadministration strategies.

In some embodiments, an anti-TNFRSF25 antibody or antigen bindingfragment as provided herein can be used during an in vitro assay ormanufacturing process as a method for stimulating proliferation of tumorinfiltrating lymphocytes isolated from a cancer patient, or to stimulateproliferation of chimeric antigen receptor expressing T cells beingexpanded in vitro and intended for subsequent infusion for the treatmentof a cancer patient.

Also provided herein are articles of manufacture containing an antibodyor antigen binding fragment as described herein, or a pharmaceuticalcomposition containing the antibody or antigen binding fragment. Theantibody or pharmaceutical composition can be within a container (e.g.,a bottle, vial, or syringe). The article of manufacture also can includea label with directions for reconstituting and/or using the antibody,antigen binding fragment, or composition. In some embodiments, anarticle of manufacture can include one or more additional items (e.g.,one or more buffers, diluents, filters, needles, syringes, and/orpackage inserts with further instructions for use). An article ofmanufacture also can include at least one additional agent for treatingcancer. For example, an article of manufacture as provided herein cancontain an agent that targets CTLA-4, PD-1, PD-L1, LAG-3, Tim-3,TNFRSF4, TNFRSF9, TNFRSF18, CD27, CD39, CD47, CD73, or CD278. In someembodiments, an article of manufacture can contain an A2A receptorantagonist or a TGF-beta antagonist. In some embodiments, an article ofmanufacture can include a B7 family costimulatory molecule (e.g., CD28or CD278) or a TNF receptor superfamily costimulatory molecule (e.g.,TNFRSF4, TNFRSF9, or TNFRSF18), a chemotherapeutic agent, or ananti-tumor vaccine composition.

The invention will be further described in the following examples, whichdo not limit the scope of the invention described in the claims.

EXAMPLES Example 1—Functional Activity of Human PTX-25

P815 cells, or P815 cells expressing human TNFRSF25, were exposed invitro to either control human IgG, human TL1A-Ig or PTX-25. TNFRSF25contains a death domain, which can lead to apoptosis in cells withactive signaling via TNFRSF25. Caspase activation can be used as amarker for cells that are undergoing apoptosis. Thus, functionalactivity of TNFRSF25 was determined by detection of caspase activationin cells expressing human TNFRSF25 and exposed to a TNFRSF25 agonist(human TL1A-Ig or PTX-25) as compared to control. Human TL1A-Ig andPTX-25, but not human IgG, led to caspase activation in P815 cellsexpressing human TNFRSF25, but not in P815 cells alone (FIG. 1). Thisassay also was performed using the various humanized constructs outlinedherein. These data demonstrated an inverse relationship between theaffinity of binding as determined by surface plasmon resonance and thefunctional activity as determined by caspase activation for thehumanized constructs (FIG. 2 and TABLE 1).

Example 2—Binding of PTX-25 to Human TNFRSF25-Fc

The binding of PTX-25 to human TNFRSF25-Fc was detected and quantifiedusing an enzyme linked immunosorbent assay (FIG. 3).

TABLE 1 EC50 (nM) WBP330BMK1 19.58 WBP330.hAb6.35800 90.46WBP330.hAb7.35806 90.44 WBP330.hAb2.35816 60.22 WBP330.hAb3.35822 62.57WBP330.hAb4.35826 59.97 WBP330.hAb8.36811 89.07 WBP330.hAb1.36558 71.51WBP330.cAb1.hIgG1(35783) 71.38

Example 3—PTX-25 Amino Acid Sequences

Hybridoma sequencing yielded one hamster VH and one hamster VL (lambda)sequence. Protein sequences, including FW and CDR regions, are shownbelow. CDR definitions are Kabat with the exception of VH CDR1, whichwas defined using IMGT definition.

Pre-humanized Parental PTX-25 VH: (SEQ ID NO: 1)EVQLVESGGGLSQPGNSLQLSCEASGFTFSNHDLNWVRQAPGKGLEWVAYISSASGLISYADAVRGRFTISRDNAKNSLFLQMNNLKSEDTAMYYCARDPPYSGLYALDFWGQGTQVTVSS FW1: (SEQ ID NO: 3) EVQLVESGGGLSQPGNSLQLSCEASCDR1: (SEQ ID NO: 4) GFTFSNHDLN FW2: (SEQ ID NO: 5) WVRQAPGKGLEWVA CDR2:(SEQ ID NO: 6) YISSASGLISYADAVRG FW3: (SEQ ID NO: 7)RFTISRDNAKNSLFLQMNNLKSEDTAMYYCAR CDR3: (SEQ ID NO: 8) DPPYSGLYALDF FW4:(SEQ ID NO: 9) WGQGTQVTVSS Pre-humanized Parental PTX-25 VL:(SEQ ID NO: 2) QPVLTQSPSASASLSGSVKLTCTLSSELSSYTIVWYQQRPDKAPKYVMYLKSDGSHSKGDGIPDRFSGSSSGAHRYLSISNVQSEDDATYFCGAGYTLAG QYGWVFGSGTKVTVL FW1:(SEQ ID NO: 10) QPVLTQSPSASASLSGSVKLTC CDR1: (SEQ ID NO: 11)TLSSELSSYTIV FW2: (SEQ ID NO: 12) WYQQRPDKAPKYVMY CDR2: (SEQ ID NO: 13)LKSDGSHSKGD FW3 (SEQ ID NO: 14) GIPDRFSGSSSGAHRYLSISNVQSEDDATYFC CDR3:(SEQ ID NO: 15) GAGYTLAGQYGWV FW4: (SEQ ID NO: 16) FGSGTKVTVL

Example 4—Humanization of PTX-25

Four humanized VH-genes were designed using homologous frameworks ofIGHV3-7*03 and IGHV3-48*03 human germ line genes. The amino acid afterthe Cys in the FW1 region was wobbled between human and mouse sequences(E and A), to better support CDR1 conformation. Two humanized VL-geneswere designed using homologous frameworks of IGLV4-60*03 and IGLV4-69*01human germ line genes. The scheme for humanization is illustrated inFIGS. 4A-B. The humanized V-genes were back-translated, codon optimized,and synthesized by GeneScript Custom Gene Synthesis. Seventeenantibodies, including one chimeric antibody and sixteen humanizedantibodies (8 IgG1 and 8 IgG4), were expressed in 293F cells. Culturesupernatants containing antibodies were harvested and purified usingProtein A chromatography. Nucleic acid and encoded amino acid sequencesfollow.

Parental clone VH regions (79.6% human) DNA: (SEQ ID NO: 34)GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTATCACAGCCTGGAAATTCCCTGCAACTCTCCTGTGAGGCCTCTGGATTCACCTTCAGTAATCATGATTTGAACTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCGCATACATTAGTAGTGCTAGTGGTCTTATCTCTTATGCCGATGCTGTGAGGGGCCGGTTCACCATCTCCAGAGACAACGCCAAGAACTCACTGTTCCTACAAATGAACAATCTCAAGTCTGAGGACACAGCCATGTATTACTGTGCAAGAGATCCTCCATATAGCGGTCTCTATGCTCTGGATTTCTGGGGTCAAGGGA CCCAAGTCACCGTCTCCTCAAmino acid: (SEQ ID NO: 1) EVQLVESGGGLSQPGNSLQLSCEASGFTFSNHDLNWVRQAPGKGLEWVAYISSASGLISYADAVRGRFTISRDNAKNSLFLQMNNLKSEDTAMYYCARDPPYSGLYALDFWGQGTQVTVSS FW1: (SEQ ID NO: 3)EVQLVESGGGLSQPGNSLQLSCEAS CDR1:  (SEQ ID NO: 4) GFTFSNHDLN FW2: (SEQ ID NO: 5) WVRQAPGKGLEWVA CDR2: (SEQ ID NO: 6) YISSASGLISYADAVRGFW3: (SEQ ID NO: 7) RFTISRDNAKNSLFLQMNNLKSEDTAMYYCAR CDR3:(SEQ ID NO: 8) DPPYSGLYALDF FW4: (SEQ ID NO: 9) WGQGTQVTVSSIGHV3-7*03 Clone 1 (88.8% human) DNA: (SEQ ID NO: 35)GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTAGTCCAGCCTGGAGGGTCCCTGAGACTCTCCTGTGAGGCCTCTGGATTCACCTTCAGTAATCATGATTTGAACTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCGCATACATTAGTAGTGCTAGTGGTCTTATCTCTTATGCCGATGCTGTGAGGGGCCGGTTCACCATCTCCAGAGACAACGCCAAGAACTCACTGTATCTACAAATGAACAGCCTCAGAGCCGAGGACACAGCCGTGTATTACTGTGCAAGAGATCCTCCATATAGCGGTCTCTATGCTCTGGATTTCTGGGGTCAAGGGA CCCAAGTCACCGTCTCCTCAAmino acid: (SEQ ID NO: 17) EVQLVESGGGLVQPGGSLRLSCEASGFTFSNHDLNWVRQAPGKGLEWVAYISSASGLISYADAVRGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCARDPPYSGLYALDFWGQGTQVTVSS FW1: (SEQ ID NO: 18)EVQLVESGGGLVQPGGSLRLSCEAS CDR1: (SEQ ID NO: 4) GFTFSNHDLN FW2:(SEQ ID NO: 19) WVRQAPGKGLEWVA CDR2: (SEQ ID NO: 6) YISSASGLISYADAVRGFW3: (SEQ ID NO: 20) RFTISRDNAKNSLYLQMNSLRAEDTAVYYCAR CDR3:(SEQ ID NO: 8) DPPYSGLYALDF FW4: (SEQ ID NO: 9) WGQGTQVTVSSIGHV3-7*03 Clone 2 (87.8% human) DNA: (SEQ ID NO: 36)GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTAGTCCAGCCTGGAGGGTCCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACCTTCAGTAATCATGATTTGAACTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCGCATACATTAGTAGTGCTAGTGGTCTTATCTCTTATGCCGATGCTGTGAGGGGCCGGTTCACCATCTCCAGAGACAACGCCAAGAACTCACTGTATCTACAAATGAACAGCCTCAGAGCCGAGGACACAGCCGTGTATTACTGTGCAAGAGATCCTCCATATAGCGGTCTCTATGCTCTGGATTTCTGGGGTCAAGGGA CCCAAGTCACCGTCTCCTCAAmino acid: (SEQ ID NO: 21) EVQLVESGGGLVQPGGSLRLSCAASGFTFSNHDLNWVRQAPGKGLEWVAYISSASGLISYADAVRGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCARDPPYSGLYALDFWGQGTQVTVSS FW1: (SEQ ID NO: 22)EVQLVESGGGLVQPGGSLRLSCAAS CDR1: (SEQ ID NO: 4) GFTFSNHDLN FW2:(SEQ ID NO: 19) WVRQAPGKGLEWVA CDR2: (SEQ ID NO: 6) YISSASGLISYADAVRGFW3: (SEQ ID NO: 20) RFTISRDNAKNSLYLQMNSLRAEDTAVYYCAR CDR3:(SEQ ID NO: 8) DPPYSGLYALDF FW4: (SEQ ID NO: 9) WGQGTQVTVSSIGHV3-48*03 Clone 1 (85.7% human) DNA: (SEQ ID NO: 37)GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTAGTCCAGCCTGGAGGGTCCCTGAGACTCTCCTGTGAGGCCTCTGGATTCACCTTCAGTAATCATGATTTGAACTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCATACATTAGTAGTGCTAGTGGTCTTATCTCTTATGCCGATGCTGTGAGGGGCCGGTTCACCATCTCCAGAGACAACGCCAAGAACTCACTGTATCTACAAATGAACAGCCTCAGAGCCGAGGACACAGCCGTGTATTACTGTGCAAGAGATCCTCCATATAGCGGTCTCTATGCTCTGGATTTCTGGGGTCAAGGGA CCCAAGTCACCGTCTCCTCAAmino acid: (SEQ ID NO: 23) EVQLVESGGGLVQPGGSLRLSCEASGFTFSNHDLNWVRQAPGKGLEWVSYISSASGLISYADAVRGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCARDPPYSGLYALDFWGQGTQVTVSS  FW1: (SEQ ID NO: 18)EVQLVESGGGLVQPGGSLRLSCEAS CDR1: (SEQ ID NO: 4) GFTFSNHDLN FW2:(SEQ ID NO: 24) WVRQAPGKGLEWVS CDR2: (SEQ ID NO: 6) YISSASGLISYADAVRGFW3: (SEQ ID NO: 42) RFTISRDNAKNSLYLQMNSLRAEDTAVYYCAR CDR3:(SEQ ID NO: 8) DPPYSGLYALDF FW4: (SEQ ID NO: 9) WGQGTQVTVSSIGHV3-48*03 Clone 2 (84.7% human) DNA: (SEQ ID NO: 38)GAGGTGCAGCTGGTGGAGTCTGGGGGAGGCTTAGTCCAGCCTGGAGGGTCCCTGAGACTCTCCTGTGCAGCCTCTGGATTCACCTTCAGTAATCATGATTTGAACTGGGTCCGCCAGGCTCCAGGGAAGGGGCTGGAGTGGGTCTCATACATTAGTAGTGCTAGTGGTCTTATCTCTTATGCCGATGCTGTGAGGGGCCGGTTCACCATCTCCAGAGACAACGCCAAGAACTCACTGTATCTACAAATGAACAGCCTCAGAGCCGAGGACACAGCCGTGTATTACTGTGCAAGAGATCCTCCATATAGCGGTCTCTATGCTCTGGATTTCTGGGGTCAAGGGA CCCAAGTCACCGTCTCCTCAAmino acid: (SEQ ID NO: 25) EVQLVESGGGLVQPGGSLRLSCAASGFTFSNHDLNWVRQAPGKGLEWVSYISSASGLISYADAVRGRFTISRDNAKNSLYLQMNSLRAEDTAVYYCARDPPYSGLYALDFWGQGTQVTVSS FW1: (SEQ ID NO: 22)EVQLVESGGGLVQPGGSLRLSCAAS CDR1: (SEQ ID NO: 4) GFTFSNHDLN FW2:(SEQ ID NO: 24) WVRQAPGKGLEWVS CDR2: (SEQ ID NO: 6) YISSASGLISYADAVRGFW3: (SEQ ID NO: 42) RFTISRDNAKNSLYLQMNSLRAEDTAVYYCAR CDR3:(SEQ ID NO: 8) DPPYSGLYALDF FW4: (SEQ ID NO: 9) WGQGTQVTVSSParental clone VL regions (70.6% human) DNA: (SEQ ID NO: 39)CAACCTGTGTTGACTCAGTCACCCTCTGCCTCTGCCTCCCTGAGTGGCTCAGTCAAACTCACCTGCACCCTGAGTAGTGAACTCAGCTCCTACACCATAGTATGGTACCAGCAACGTCCAGACAAGGCTCCCAAGTATGTGATGTACCTTAAGAGTGATGGAAGCCACAGCAAAGGAGATGGGATCCCTGATCGCTTCTCTGGCTCCAGCTCTGGGGCTCATCGCTACTTAAGCATCTCCAATGTCCAGTCTGAAGATGATGCTACCTATTTCTGTGGTGCAGGTTATACCCTTGCTGGACAATATGGGTGGGTGTTCGGTTCAGGCACCAAAGTGACTGTCC TA Amino acid:(SEQ ID NO: 2) QPVLTQSPSASASLSGSVKLTCTLSSELSSYTIVWYQQRPDKAPKYVMYLKSDGSHSKGDGIPDRFSGSSSGAHRYLSISNVQSEDDATYFCGAGYTLAGQYGWVFGSGTKVTVL FW1: (SEQ ID NO: 10) QPVLTQSPSASASLSGSVKLTC CDR1:(SEQ ID NO: 11) TLSSELSSYTIV FW2: (SEQ ID NO: 12) WYQQRPDKAPKYVMY CDR2:(SEQ ID NO: 13) LKSDGSHSKGD FW3: (SEQ ID NO: 14)GIPDRFSGSSSGAHRYLSISNVQSEDDATYFC CDR3: (SEQ ID NO: 15) GAGYTLAGQYGWVFW4: (SEQ ID NO: 16) FGSGTKVTVL IGLV4-60*03 Clone (89.1% human) DNA:(SEQ ID NO: 40) CAACCTGTGTTGACTCAGTCATCCTCTGCCTCTGCCTCCCTGGGATCCTCAGTCAAACTCACCTGCACCCTGAGTAGTGAACTCAGCTCCTACACCATAGTATGGCATCAGCAACAGCCAGGGAAGGCTCCCCGGTATTTGATGTACCTTAAGAGTGATGGAAGCCACAGCAAAGGAGATGGGGTTCCTGATCGCTTCTCTGGCTCCAGCTCTGGGGCTGACCGCTACTTAACCATCTCCAATCTCCAGTCTGAAGATGAGGCTGATTATTACTGTGGTGCAGGTTATACCCTTGCTGGACAATATGGGTGGGTGTTCGGTTCAGGCACCAAAGTGACTGTCCT A Amino acid:(SEQ ID NO: 26) QPVLTQSSSASASLGSSVKLTCTLSSELSSYTIVWHQQQPGKAPRYLMYLKSDGSHSKGDGVPDRFSGSSSGADRYLTISNLQSEDEADYYCGAGYTLAGQYGWVFGSGTKVTVL FW1: (SEQ ID NO: 27) QPVLTQSSSASASLGSSVKLTCCDR1: (SEQ ID NO: 11) TLSSELSSYTIV FW2: (SEQ ID NO: 28) WHQQQPGKAPRYLMYCDR2: (SEQ ID NO: 13) LKSDGSHSKGD FW3: (SEQ ID NO: 29)GVPDRFSGSSSGADRYLTISNLQSEDEADYYC CDR3: (SEQ ID NO: 15) GAGYTLAGQYGWVFW4: (SEQ ID NO: 16) FGSGTKVTVL IGLV4-69*01 Clone (94.6% human) DNA:(SEQ ID NO: 41) CAACTTGTGTTGACTCAGTCACCCTCTGCCTCTGCCTCCCTGGGAGCCTCAGTCAAACTCACCTGCACCCTGAGTAGTGAACTCAGCTCCTACACCATAGTATGGCATCAGCAACAGCCAGAGAAGGGCCCCCGGTATTTGATGTACCTTAAGAGTGATGGAAGCCACAGCAAAGGAGATGGGATCCCTGATCGCTTCTCTGGCTCCAGCTCTGGGGCTGAGCGCTACTTAACCATCTCCAGCCTCCAGTCTGAAGATGAGGCTGATTATTACTGTGGTGCAGGTTATACCCTTGCTGGACAATATGGGTGGGTGTTCGGTTCAGGCACCAAAGTGACTGTCCT A Amino acid:(SEQ ID NO: 30) QLVLTQSPSASASLGASVKLTCTLSSELSSYTIVWHQQQPEKGPRYLMYLKSDGSHSKGDGIPDRFSGSSSGAERYLTISSLQSEDEADYYCGAGYTLAGQYGWVFGSGTKVTVL FW1: (SEQ ID NO: 31) QLVLTQSPSASASLGASVKLTCCDR1: (SEQ ID NO: 11) TLSSELSSYTIV FW2: (SEQ ID NO: 32) WHQQQPEKGPRYLMYCDR2: (SEQ ID NO: 13) LKSDGSHSKGD FW3: (SEQ ID NO: 33)GIPDRFSGSSSGAERYLTISSLQSEDEADYYC CDR3: (SEQ ID NO: 15) GAGYTLAGQYGWVFW4: (SEQ ID NO: 16) FGSGTKVTVL

Example 5—In Vitro Stimulation of CD4+ and CD8+ T Cell Proliferation byPTX-25

Human T cells were purified by gradient centrifugation and plated in thepresence of plate-bound anti-human CD3 antibody and IL-2. PTX-25 wasadded, and the proliferation of human CD4+ and CD8+ T cells was detectedusing flow cytometry following incorporation of Click-Edu reagent invitro. Graphs plotting the in vitro stimulation of human CD4+ and CD8+ Tcell proliferation by PTX-25 are shown in FIG. 5. Left panel, CD4+cells; right panel, CD8+ cells.

Example 6—In Vitro Binding Activity of Humanized TNFRSF25 AntibodyConstructs to Human TNFRSF25

The indicated humanized TNFRSF25 antibodies were incubated with P815cells expressing human TNFRSF25 at the indicated antibodyconcentrations. Binding of each antibody to the cells was then detectedby flow cytometry. The mean fluorescence intensity of binding isindicated on the y-axis for each concentration of antibody indicated onthe x-axis (FIG. 6 and TABLE 2).

TABLE 2 Bmax Kd (μM) WBP330BMK1 246.0 0.07354 WBP330.hAb6.35800 255.50.1014 WBP330.hAb7.35806 245.1 0.07578 WBP330.hAb2.35816 250.4 0.08871WBP330.hAb3.35822 242.1 0.07678 WBP330.hAb4.35826 251.3 0.1168WBP330.hAb8.36811 225.9 0.07046 WBP330.hAb1.36558 238.9 0.07299

Example 7—Affinity of Humanized TNFRSF25 Antibodies to Human TNFRSF25

Affinity of the indicated humanized TNFRSF25 antibodies was determinedby surface plasmon resonance (SPR) using the ProteOn method (FIG. 7 andTABLE 3).

Example 8—In Vitro Caspase Release

Caspase release induced by BMK1, chimeric antibody cAb1.hIgG1 (35783),and the most potent humanized antibody hAb2(35816) was tested. ChimericcAb1.hIgG1 (35783) and humanized hAb2 (35816) induced caspase activitieswith the EC₅₀ of 121.4 and 68.2 ng/ml, respectively, both of which werehigher than the EC₅₀ of BMK1 (19.2 ng/ml; FIG. 8). The maximal caspaseactivity induced by the engineered antibodies was significantly lowerthan by the original 4C12-A5 MAb. The significant difference in in vitropotencies of 4C12-A5 and cAb1.hIgG1 indicated that antibody constantregion plays a role in modulating agonistic activity by theseantibodies. The in vitro potency of humanized hAb2 was within 3-4 foldof the original hamster MAb. The hTL1A-hFc chimera, which is the ligandfor TNFRSF25, induced caspase activity with an EC₅₀ of 282.5 ng/ml.

TABLE 3 Bivalent Analyte Ka Kd KD Rmax Ka2 Kd2 Chi2 Ligand Analyte(1/Ms) (1/s) (M) (RU) (1/RUs) (1/s) (RU) WBP330.hProl.ECD.hF WBP330BMK19.90E+04 2.52E−02 2.54E−07 109.18 2.17E−04 9.04E−04 4.72WBP330.cAB1.hIgG1 (35783) 9.90E+04 5.76E−03 5.81E−08 83.06 3.52E−042.24E−03 5.62 WBP330.hAb.35800 8.79E+04 1.18E−02 1.34E−07 61.49 1.03E−041.09E−03 4.43 hAb6 WBP330.hAb.35806 8.23E+04 1.29E−02 1.57E−07 57.871.35E−04 1.49E−03 4.34 hAb7 WBP330.hAb.35816 8.90E+04 6.32E−03 7.09E−0877.57 2.38E−04 1.28E−03 5.07 hAb2 WBP335.hAb.35822 7.39E+04 8.08E−031.09E−07 86.73 2.70E−04 1.67E−03 5.48 hAb3 WBP335.hAb.35826 7.26E+041.98E−02 2.73E−07 107.63 2.12E−04 1.07E−03 6.02 hAb4 WBP335.hAb.368117.13E+04 1.49E−02 2.08E−07 63.40 1.52E−04 1.68E−03 4.53 hAb8WBP330.hAb.36558 7.61E+04 1.10E−02 1.44E−07 95.81 2.81E−04 1.36E−03 6.33hAb1

Example 9—Antibody-Dependent Cell-Mediated Cytotoxicity

The antibody-dependent cell-mediated cytotoxicity (ADCC) of chimeric andhumanized antibodies was measured by incubating target cells with PBMCsfor 6 hours with an effector/target ratio of 50:1, using indicated IgGconcentrations ranging from 10 ug/ml to 0.01 ng/ml. The maximal lysisrate reached 40%, and the EC₅₀ for antibodies ranged from 47 ng/ml to240 ng/ml (FIG. 9; TABLE 4). No significant difference was observedbetween chimeric and humanized antibodies.

TABLE 4 EC50 (ng/ml) Top % cAb1 (35783) 88.3 40.5 hAb1 (36558) 47.3 45.6hAb2 (35816) 56.3 44.6 hAb3 (35822) 79.0 46.0 hAb4 (35826) 60.1 44.2hAb5 (35812) 148.3 47.8 hAb6 (35800) 199.5 43.5 hAb7 (35806) 239.8 45.6hAb8 (36811) 85.1 34.6

Other Embodiments

It is to be understood that while the invention has been described inconjunction with the detailed description thereof, the foregoingdescription is intended to illustrate and not limit the scope of theinvention, which is defined by the scope of the appended claims. Otheraspects, advantages, and modifications are within the scope of thefollowing claims.

1-46. (canceled)
 47. A method of treating a tumor in a subject,comprising administering to a subject a composition comprising ananti-tumor necrosis factor superfamily receptor 25 (TNFRSF25) antibody,the anti-TNFRSF25 antibody comprising: (a) a heavy chain comprising aheavy chain variable region comprising a CDR1 sequence as set forth inSEQ ID NO: 4, a CDR2 sequence as set forth in SEQ ID NO: 6, and a CDR3sequence as set forth in SEQ ID NO: 8; and (b) a light chain comprisingalight chain variable region comprising a CDR1 sequence as set forth inSEQ ID NO: 11, a CDR2 sequence as set forth in SEQ ID NO: 13, and a CDR3sequence as set forth in SEQ ID NO:
 15. 48. The method of claim 47,wherein the heavy chain variable region comprises the amino acidsequence having at least 90% identity to SEQ ID NO:
 1. 49. The method ofclaim 47, wherein the light chain variable region comprises the aminoacid sequence having at least 90% identity to SEQ ID NO:
 2. 50. Themethod of claim 47, wherein the heavy constant region of the antibody isselected from human IgG1, IgG2, IgG3, and IgG4.
 51. The method of claim50, wherein the heavy constant region is from human IgG4.
 52. The methodof claim 47, wherein the method further comprises administering anadditional agent for treating cancer.
 53. The method of claim 52,wherein the additional agent comprises an agent that targets CTLA-4,PD-1, PD-L1, LAG-3, Tim-3, TNFRSF4, TNFRSF9, TNFRSF18, CD27, CD39, CD47,CD73, or CD278.
 54. The method of claim 52, wherein the additional agentcomprises a TNF receptor superfamily costimulatory molecule.
 55. Themethod of claim 52, wherein the additional agent comprises chimericantigen receptor-transfected T cells or expanded tumor infiltratinglymphocytes for use in an adoptive T cell therapy.
 56. The method ofclaim 52, wherein the additional agent comprises a chemotherapeuticagent.